NEEDLE SPECIALTY PRODUCTS

FDA Device Registration & Listing · Boyle, MS, US · Registration 1000112137

Public Record Device Listing Expiry Year: 2026 AvaSpecs displays structured public-record fields for easier browsing and citation.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1000112137
FEI Number
1000112137
Entity Name
NEEDLE SPECIALTY PRODUCTS
City/State/Country
Boyle, MS, US
Establishment Address
600 Highway 446, Boyle, MS 38730, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Needle Specialty Products (Owner Number: 10042203)
Owner / Operator Contact Address
600 Highway 446, Boyle, MS 38730, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dualok

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GDF Guide, Needle, Surgical General, Plastic Surgery Class 1 878.4800 2012-10-31

Official Correspondent

Gerald Smith

US Agent Details

No US Agent registered (Local establishment).

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000112137. Last updated year: 2026. Please use registration number 1000112137 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
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